ATP7b Antibody - BSA Free
Novus Biologicals | Catalog # NB100-361
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Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for ATP7b Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence: ATP7b Antibody [NB100-361]
Immunocytochemistry/Immunofluorescence: ATP7b Antibody [NB100-361] - Caco-2 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.05% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti-ATP7b Antibody NB100-361 at 2 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.Western Blot: ATP7b Antibody [NB100-361] -
Western Blot: ATP7b Antibody [NB100-361] - Effects & mechanism of action of CASIN on melphalan-resistant MM cells. (A) CASIN reduces Cdc42 activity (Cdc42-GTP) but not Rac1 activity (Rac1-GTP). Melphalan-sensitive MM cells (S) were treated with Vehicle or CASIN (5 μM) for 8 h. Cdc42 & Rac1 activities were measured using pull-down assay. (B) CASIN (5 μM) inhibits proliferation of both S & melphalan-resistant (LR5) MM cells. **P < 0.01 vs. S-Vehicle; ##P < 0.01 vs. LR5-Vehicle. (C) CASIN (5 μM) preferentially causes apoptosis of melphalan-resistant MM cells. S & LR5 cells were treated with or without CASIN or melphalan (Mel, 25 μM) or both for 2 days. Annexin V+ cells were analyzed using flow cytometry. **P < 0.01. (D–F) Mechanism of action of CASIN on melphalan-resistant MM cells. (D) Cdc42 activity & expression are increased in LR5 cells compared to that in S cells. Cdc42 activity was measured using pull-down assay. beta -Actin was used as loading control. Vertical lines indicate the gel lanes being switched in position from the original blots. (E) CASIN (5 μM) decreases melphalan-induced FANCD2 mono-ubiquitination (Ub-FANCD2) in LR5 but not in S cells. S & LR5 cells were treated with or without CASIN, Mel (25 μM), or both for 16 h. FANCD2 was detected using western blotting. beta -Actin was used as loading control. (F) CASIN sensitizes melphalan-resistant but not -sensitive MM cells to melphalan-induced DNA damage. gamma H2A histone family member X-positive ( gamma H2AX+) cells were detected using flow cytometry. **P < 0.01. Error bars represent means ± SD of triplicates & data are representative of three independent experiments. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/31632904), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for ATP7b Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence
Western Blot
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Background: ATP7b
Alternate Names
Gene Symbol
Additional ATP7b Products
Product Documents for ATP7b Antibody - BSA Free
Certificate of Analysis
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Product Specific Notices for ATP7b Antibody - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for ATP7b Antibody - BSA Free
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Protocols
View specific protocols for ATP7b Antibody - BSA Free (NB100-361):
Immunohistochemistry Procedure
Cell Preparation (At least 108 cells were used per block)
1. Harvesting cells:
A. Trypsinization
B. 15 minute centrifugation at 2,500 RPM
C. PBS rinse
D. 15 minute centrifugation at 2,500 RPM
2. Suspend cells in 10 ml of 10% formaldehyde in PBS, overnight @ RT.
3. Centrifuge cells at 2,500 RPM for 10 minutes.
4. Resuspend cells in 10 ml of 70% ethanol.
5. Centrifuge cells at 2,500 RPM and taken into 70% ethanol.
Cell Staining
1. Ribbon Thickness: 5 um
2. Deparaffination Agent: Xylin
3. Hydration: Ethanol in PBS
4. Blocking:
A. endogeneous peroxidase: 0.3% H2O2 in PBS for 10 minutes
B. endogeneous protein: 1% BSA for 20 minutes
6. Primary antibody, polyclonal anti-ATP7b (NB 100-361): 1:500, overnight @ 4 degrees Celcius
7. Secondary antibody, anti-rabbit (HRP): (dilute per manufacturer recommendation), 30 minutes @ RT
8. Wash 3x 15 minutes
9. Chromogen: AEC
10. Counterstain: Mayers hematoxylin
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars